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FDADecember 19, 2018device

ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.

What to do

FDA enforcement status: Terminated

Brands named

arjohuntleigh magogarjohuntleigh

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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